Lymphatic filariasis

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ORPHA:2035B74.0B74.1B74.2
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28Specialists8Treatment centers

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UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
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Overview

Lymphatic filariasis, also commonly known as elephantiasis, is a tropical infectious disease caused by parasitic roundworms (nematodes) that are spread to humans through mosquito bites. Three species of worms can cause this disease: Wuchereria bancrofti (the most common), Brugia malayi, and Brugia timori. When an infected mosquito bites a person, tiny larvae enter the body and travel to the lymphatic system, where they grow into adult worms over several months. These adult worms can live for years inside the lymph vessels, causing damage and blockage to the lymphatic system, which is a key part of the body's immune defense and fluid drainage. Many people with lymphatic filariasis have no visible symptoms for years, even though the worms are silently damaging the lymphatic system and kidneys. Over time, the disease can cause dramatic swelling of the limbs (lymphedema), most commonly the legs, and swelling of the genitals (hydrocele in men). In its most severe form, called elephantiasis, the skin becomes thickened and hardened, and the affected limbs become extremely enlarged. Patients are also more prone to painful bacterial skin infections in the swollen areas. The disease can cause significant disability and social stigma. Treatment involves antiparasitic medications to kill the worms, including diethylcarbamazine (DEC), ivermectin, and albendazole, which are used in mass drug administration programs in affected regions. For people who already have chronic swelling, careful hygiene, skin care, elevation of affected limbs, exercise, and sometimes surgery (especially for hydrocele) can help manage symptoms. While the infection itself can be treated and prevented, the chronic damage to the lymphatic system is often irreversible, making early treatment and prevention critically important.

Key symptoms:

Swelling of the legs (lymphedema)Swelling of the armsSwelling of the genitals, especially the scrotum in men (hydrocele)Thickened, hardened skin on affected limbsRecurrent bacterial skin infections in swollen areasFever and chills during acute episodesPain and tenderness in the groin or armpit lymph nodesSwollen lymph nodesMilky or cloudy urine (chyluria)Fatigue and general feeling of being unwellDifficulty walking due to leg swellingSkin rashes or itchingBreast swelling in women

Clinical phenotype terms (33)— hover any for plain English
Predominantly lower limb lymphedemaHP:0003550Abnormality of the lymphatic systemHP:0100763LymphadenitisHP:0002840Circulating immune complexesHP:0012224Severely increased total eosinophil countHP:0032061Hydrocele testisHP:0000034Abnormal scrotum morphologyHP:0000045Abnormal lung morphologyHP:0002088Opportunistic infectionHP:0031690
Age of Onset

Variable

Can begin at different ages, from infancy through adulthood

Orphanet ↗NORD ↗

Treatments

No FDA-approved treatments are currently listed for Lymphatic filariasis.

View clinical trials →

No actively recruiting trials found for Lymphatic filariasis at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Lymphatic filariasis community →

Specialists

Showing 25 of 28View all specialists →
PP
Peter U Fischer, PhD
Specialist
PI on 2 active trials
CP
Christopher L King, MD PhD
Specialist
PI on 1 active trial
GM
Gary J Weil, MD
BELLEVUE, WA
Specialist
PI on 3 active trials1 Lymphatic filariasis publication
NM
Nicholas O Opoku, MD
Specialist
PI on 1 active trial
EM
Eric Ottesen, MD
WASHINGTON, DC
Specialist
PI on 3 active trials
MM
Michel Mandro, MD
Specialist
PI on 1 active trial
GM
Gary Weil, MD
BELLEVUE, WA
Specialist
PI on 5 active trials1 Lymphatic filariasis publication
KM
Karsor Kollie, MSc
Specialist
PI on 1 active trial
TM
Tony Ukety, MD, DO, MPH
Specialist
PI on 2 active trials
PP
Peter Fischer, PhD
Specialist
PI on 1 active trial
TM
Thomas B Nutman, M.D.
BETHESDA, MD
Specialist
PI on 7 active trials
LM
Lucy John, MD
Specialist
PI on 1 active trial1 Lymphatic filariasis publication
CP
Christopher King, MD PhD
Specialist
PI on 1 active trial
PP
Patrick Kpanyen, PhD
Specialist
PI on 1 active trial
NM
Nina O Nielsen, Ms.c
NORTHBROOK, IL
Specialist
PI on 1 active trial
RM
Roopal Kundu, MD
CHICAGO, IL
Specialist
PI on 1 active trial
AM
Amy D Klion, M.D.
BETHESDA, MD
Specialist
PI on 8 active trials
JD
Jeremy Dennison
Specialist
PI on 1 active trial3 Lymphatic filariasis publications
RP
Rachel L Pullan, PhD
Specialist
PI on 2 active trials
JM
Jeremy Dennison, PhD MBChB
Specialist
PI on 1 active trial
SM
Samba O Sow, MD, MPH
Specialist
PI on 1 active trial
AM
Asanta M Asio, Msc
Specialist
PI on 1 active trial
DP
Dziedzom K de Souza, PhD
Specialist
PI on 1 active trial
AM
Aboulaye Miete, MD
Specialist
PI on 1 active trial1 Lymphatic filariasis publication
RP
Richard Phillips O Phillips, MBChB, PhD
Specialist
PI on 1 active trial

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Lymphatic filariasis.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Lymphatic filariasis

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Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Questions for your doctor

Bring these to your next appointment

  • Q1.What stage is my lymphatic filariasis, and how much damage has already occurred to my lymphatic system?,Which antiparasitic medication is best for my situation, and how long will I need to take it?,What daily care routine should I follow to prevent my swelling from getting worse?,How can I recognize a bacterial skin infection early, and what should I do if one occurs?,Are there surgical options that could help with my swelling or hydrocele?,How can I protect my family members from getting infected?,Are there mental health or support resources available for people living with this condition?

Common questions about Lymphatic filariasis

What is Lymphatic filariasis?

Lymphatic filariasis, also commonly known as elephantiasis, is a tropical infectious disease caused by parasitic roundworms (nematodes) that are spread to humans through mosquito bites. Three species of worms can cause this disease: Wuchereria bancrofti (the most common), Brugia malayi, and Brugia timori. When an infected mosquito bites a person, tiny larvae enter the body and travel to the lymphatic system, where they grow into adult worms over several months. These adult worms can live for years inside the lymph vessels, causing damage and blockage to the lymphatic system, which is a key par

Which specialists treat Lymphatic filariasis?

25 specialists and care centers treating Lymphatic filariasis are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.